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rs17035378

From SNPedia

Orientationplus
Stabilizedplus
Make rs17035378(C;C)
Make rs17035378(C;T)
Make rs17035378(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position68371823
GenePLEK
is asnp
is mentioned by
dbSNPrs17035378
ebirs17035378
HLIrs17035378
Exacrs17035378
Varsomers17035378
Maprs17035378
PheGenIrs17035378
hapmaprs17035378
1000 genomesrs17035378
hgdprs17035378
ensemblrs17035378
gopubmedrs17035378
geneviewrs17035378
scholarrs17035378
googlers17035378
pharmgkbrs17035378
gwascentralrs17035378
openSNPrs17035378
23andMers17035378
23andMe allrs17035378
SNP Nexus

SNPshotrs17035378
SNPdbers17035378
MSV3drs17035378
GWAS Ctlgrs17035378
GMAF0.4421
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20190752OA-icon.png]
Trait Celiac disease
Title Multiple common variants for celiac disease influencing immune gene expression
Risk Allele
P-val 8E-9
Odds Ratio 1.14 [1.09-1.19]